Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines
Retinoblastoma is a childhood tumor of the retina that is caused mostly by biallelic inactivation of the tumor suppressor gene RB1. To generate a research resource, we abrogated expression of RB1 in H9 hESCs by CRISPR/Cas9 induced deletion of the RB1 promoter, either on one or on both alleles. This...
Main Authors: | Hannah Döpper, Marius Horstmann, Julia Menges, Morgane Bozet, Deniz Kanber, Laura Steenpass |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2020-05-01
|
Series: | Stem Cell Research |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1873506120300830 |
Similar Items
-
Generation of heterozygous and homozygous hESC H9 sublines carrying inactivating mutations in RB1
by: Leonie Schipper, et al.
Published: (2018-12-01) -
Generation of two H1 hESC sublines carrying a heterozygous and homozygous knock-out of RB1
by: Laura Steenpass
Published: (2017-12-01) -
hESC-derived immune suppressive dendritic cells induce immune tolerance of parental hESC-derived allografts
by: Dilyana Todorova, et al.
Published: (2020-12-01) -
hESC expansion and stemness are independent of connexin forty-three-mediated intercellular communication between hESCs and hASC feeder cells.
by: Jin-Su Kim, et al.
Published: (2013-01-01) -
<i>RB1</i>-Negative Retinal Organoids Display Proliferation of Cone Photoreceptors and Loss of Retinal Differentiation
by: Deniz Kanber, et al.
Published: (2022-04-01)